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6 April 2004 | Volume 140 Issue 7 | Pages 1-4
This statement summarizes the current U.S. Preventive Services Task Force (USPSTF) recommendations on screening for coronary heart disease and the supporting scientific evidence and updates the 1996 recommendations on this topic. The complete information on which this statement is based, including evidence tables and references, is available in the background article and the systematic evidence review, available through the USPSTF Web site (http://www.preventiveservices.ahrq.gov) and through the National Guideline Clearinghouse (http://www.guideline.gov). The article and the recommendation statement are also available in print through the Agency for Healthcare Research and Quality Publications Clearinghouse (telephone, 800-358-9295; e-mail, ahrqpubs{at}ahrq.gov).
CLINICAL GUIDELINES
Screening for Coronary Heart Disease: Recommendation Statement
Summary of the Recommendations
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The U.S. Preventive Services Task Force (USPSTF) recommends against routine screening with resting electrocardiography (ECG), exercise treadmill test (ETT), or electron-beam computerized tomography (EBCT) scanning for coronary calcium for either the presence of severe coronary artery stenosis (CAS) or the prediction of coronary heart disease (CHD) events in adults at low risk for CHD events. This is a grade D recommendation. (See Appendix Table 1 for a description of the USPSTF classification of recommendations.)
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The USPSTF found inadequate evidence to determine the extent to which the added detection offered by ECG, ETT, or EBCT (beyond that obtained by ascertainment of conventional CHD risk factors) (see Clinical Considerations) would result in interventions that lead to improved CHD-related health outcomes among adults at increased risk for CHD events. Although there is limited evidence to determine the magnitude of harms from screening this population, harms from false-positive tests (that is, unnecessary invasive procedures, overtreatment, and labeling) are likely to occur. As a result, the USPSTF could not determine the balance between benefits and harms of screening this population for CHD.
Clinical Considerations
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Screening with ECG, ETT, and EBCT could potentially reduce CHD events in 2 ways: either by detecting people at high risk for CHD events who could benefit from more aggressive risk factor modification or by detecting people with existing severe CAS whose life could be prolonged by coronary artery bypass grafting (CABG) surgery. However, the evidence is inadequate to determine the extent to which people detected through screening in either situation would benefit from either type of intervention.
The consequences of false-positive tests may potentially outweigh the benefits of screening. False-positive tests are common among asymptomatic adults, especially women, and may lead to unnecessary diagnostic testing, overtreatment, and labeling.
Because the sensitivity of these tests is limited, screening could also result in false-negative results. A negative test does not rule out the presence of severe CAS or a future CHD event.
For people in certain occupations, such as pilots and heavy equipment operators (for whom sudden incapacitation or sudden death may endanger the safety of others), considerations other than the health benefit to the individual patient may influence the decision to screen for CHD.
Although some exercise programs initially screen asymptomatic participants with ETT, there is not enough evidence to determine the balance of benefits and harms of this practice.
Discussion
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Many clinicians ascertain a person's overall risk for CHD events by screening for cardiac risk factors and incorporating that information into risk prediction equations derived from the Framingham or other cohort studies (3, 4). Asymptomatic adults clearly benefit from risk factor modification proportional to their degree of CHD risk (that is, more intensive risk factor modification for people at higher risk) (5). Since those at high risk for CHD may already be receiving interventions to maximally reduce their risk for CHD events, screening may potentially be of greatest benefit to those presumed to be at intermediate risk for CHD who could be reclassified as being at high risk (and thus treated more aggressively) after additional testing. In addition to risk factor reduction, persons with symptoms of CHD who have severe CAS (defined as either triple-vessel or left main coronary artery atherosclerotic disease with poor left ventricular function) clearly benefit from CABG or percutaneous transluminal coronary angioplasty (6-8). Among the asymptomatic population, those at higher risk for CHD events have a higher prevalence of severe CAS; thus, the yield of screening is expected to be greater in this population. However, it is uncertain whether this increased yield increases the detection of people with severe CAS to an important degree and whether invasive revascularization procedures would benefit those who are asymptomatic as much as those who have symptoms of CAS.
The USPSTF reviewed the evidence as to whether supplementing the conventional CHD risk ascertainment strategy with additional screening using ECG, ETT, or EBCT, or using these 3 tests to identify people with severe CAS earlier, would lead to improved health outcomes in asymptomatic persons. The USPSTF found no randomized, controlled trials with health outcomes that examined the extent to which ECG, ETT, or EBCT scanning for coronary calcium provided additional prognostic information beyond the currently used risk factor calculations. The Task Force further found that the 3 screening testsECG, ETT, and EBCThave poor to fair accuracy in predicting CHD events.
Systematic reviews have reported that the sensitivity of resting ECG abnormalities for CHD events is low (3, 9). The prevalence of the most common ECG abnormalities (Q waves, left ventricular hypertrophy, bundle-branch blocks, and ST-segment depression) ranges from 1% to 10% (3). Only a few studies have examined ECG abnormalities in the black population. Although major ECG abnormalities may be more prevalent in black men than in white men, these abnormalities may not confer the same risk for CHD death in black men (relative risk, 1.95 [95% CI, 0.93 to 4.11]) as in white men (relative risk, 2.72 [CI, 1.47 to 5.04]) (10).
The sensitivity of ETT for the prediction of CHD events 3 to 12 years in the future ranges from 40% to 62%; the positive predictive value (PPV) ranges from 6% to 48%. The higher sensitivity of ETT reported in older studies may not be accurate because of the possibility of spectrum bias (11, 12). The prevalence of an abnormal ETT (ST-segment depression
1 mm) reportedly ranges from 5% to 25% (3). The yield of ETT in detecting severe CAS in asymptomatic middle-aged men is estimated to be 0.5% (3, 13). The PPV for future CHD in recent cohort studies (most of them conducted with asymptomatic men) is low (range, 6% to 48%) (3). Adding nuclear perfusion to ECG analysis may increase sensitivity somewhat; however, the low PPV of ETT is due mainly to the low prevalence of CHD in asymptomatic persons and cannot be corrected simply by improving test accuracy.
For patients with symptoms of CHD, EBCT has a sensitivity of 80% and a specificity of 40% for detecting angiographically demonstrated CAS (14); similar data for those who have no symptoms are lacking. A systematic review reported that higher calcium scores on EBCT were associated with higher risk for CHD events (3). This review concluded that EBCT may have a role in better defining risk for CHD events in those who have been identified as being at intermediate risk based on traditional risk factors, but no study has examined the effect of EBCT data on clinical decision making (3).
Potential harms of screening asymptomatic patients for CHD include unnecessary invasive testing (for example, coronary angiography) and "labeling" of those who have had false-positive test results. In low-risk asymptomatic populations, most positive ECG test results occur in those who will not have a CHD event in the next 5 to 10 years (3). One study reported that 71% of those without symptoms who had an abnormal ETT had no angiographically demonstrable CAS (15). While the yield of screening is low in those at low risk for CHD, the potential for harm from false-positive tests is high. The USPSTF judged that the benefits of screening people at low risk for CHD would not outweigh the potential harms.
Because of the limited sensitivity of resting ECG and the low prevalence of CHD in asymptomatic adults, a majority of CHD events will occur among those with an initially normal ECG (that is, those who test false negative) (16). The ETT can be normal or nondiagnostic in a large proportion of patients who will go on to have a CHD event, which may be explained partly by the fact that many acute CHD events result from sudden occlusion of a previously unobstructed artery segment (17).
A large study, the Multi-Ethnic Study of Atherosclerosis (MESA), is ongoing. Data from this study will help to examine the independent prognostic information derived from EBCT in the context of accurate measurement of traditional risk factors and extended follow-up (18). In the absence of such data for ECG, ETT, or EBCT, the USPSTF concluded there is insufficient evidence to recommend for or against screening for CHD.
Recommendations of Others
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Appendix
Members of the U.S. Preventive Services Task Force are Alfred O. Berg, MD, MPH, Chair (University of Washington, Seattle, Washington); Janet D. Allan, PhD, RN, CS, Vice-Chair (University of Maryland Baltimore, Baltimore, Maryland); Ned Calonge, MD, MPH (Colorado Department of Public Health and Environment, Denver, Colorado); Paul Frame, MD (Tri-County Family Medicine, Cohocton, and University of Rochester, Rochester, New York); Joxel Garcia, MD, MBA (Pan American Health Organization, Washington, DC); Russell P. Harris, MD, MPH (University of North Carolina School of Medicine, Chapel Hill, North Carolina); Mark S. Johnson, MD, MPH (University of Medicine and Dentistry of New JerseyNew Jersey Medical School, Newark, New Jersey); Jonathan D. Klein, MD, MPH (University of Rochester School of Medicine, Rochester, New York); Carol Loveland-Cherry, PhD, RN (University of Michigan, Ann Arbor, Michigan); Virginia A. Moyer, MD, MPH (University of Texas at Houston, Houston, Texas); C. Tracy Orleans, PhD (The Robert Wood Johnson Foundation, Princeton, New Jersey); Albert L. Siu, MD, MSPH (Mount Sinai School of Medicine, New York, New York); Steven M. Teutsch, MD, MPH (Merck & Co., Inc., West Point, Pennsylvania); Carolyn Westhoff, MD, MSc (Columbia University, New York, New York); and Steven H. Woolf, MD, MPH (Virginia Commonwealth University, Fairfax, Virginia). This list includes members of the Task Force at the time this recommendation was finalized. For a list of current Task Force members, go to http://www.ahrq.gov/clinic/uspstfab.htm.
Author and Article Information
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*For a list of the members of the U.S. Preventive Services Task Force, see the Appendix.
Disclaimer: The USPSTF recommendations are independent of the U.S. government. They do not represent the views of the Agency for Healthcare Research and Quality, the U.S. Department of Health and Human Services, or the U.S. Public Health Service.
Requests for Single Reprints: Reprints are available from the USPSTF Web site (http://www.preventiveservices.ahrq.gov) and in print through the Agency for Healthcare Research and Quality Publications Clearinghouse (800-358-9295).
References
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1. National Center for Health Statistics, Centers for Disease Control and Prevention, U.S. Department of Health and Human Services. Fast Stats A to Z: DeathLeading Causes. Accessed at http://www.cdc.gov/nchs/fastats/lcod.htm on 4 April 2003.
2. American Heart Association. Cardiovascular Disease Cost. Accessed at http://www.americanheart.org/presenter.jhtml?identifier=4475 on 25 November 2003.
3. Pignone M, Fowler-Brown A, Pletcher M, Tice JA. Screening for Asymptomatic Coronary Artery Disease. Systematic Evidence Review No. 22. Rockville, MD: Agency for Healthcare Research and Quality; 2003. Available at http://www.ahrq.gov/clinic/serfiles.htm.
4. Wilson PW, D'Agostino RB, Levy D, Belanger AM, Silbershatz H, Kannel WB. Prediction of coronary heart disease using risk factor categories. [PMID: 9603539] Circulation. 1998;97:1837-47.
5. 27th Bethesda Conference. Matching the Intensity of Risk Factor Management with the Hazard for Coronary Disease Events. September 14-15, 1995. J Am Coll Cardiol. 1996;27:957-1047. [PMID: 8609361].
6. Coronary artery surgery study (CASS): a randomized trial of coronary artery bypass surgery. Survival data. [PMID: 6137292] Circulation. 1983;68:939-50.
7. Parisi AF, Folland ED, Hartigan P. A comparison of angioplasty with medical therapy in the treatment of single-vessel coronary artery disease. Veterans Affairs ACME Investigators. [PMID: 1345754] N Engl J Med. 1992;326:10-6.[Abstract]
8. Coronary angioplasty versus coronary artery bypass surgery: the Randomized Intervention Treatment of Angina (RITA) trial. [PMID: 8094826] Lancet. 1993;341:573-80.[Medline]
9. Ashley EA, Raxwal V, Froelicher V. An evidence-based review of the resting electrocardiogram as a screening technique for heart disease. [PMID: 11533927] Prog Cardiovasc Dis. 2001;44:55-67.[Medline]
10. Kannel WB, Anderson K, McGee DL, Degatano LS, Stampfer MJ. Nonspecific electrocardiographic abnormality as a predictor of coronary heart disease: the Framingham Study. [PMID: 3812192] Am Heart J. 1987;113:370-6.[Medline]
11. Ashley EA, Myers J, Froelicher V. Exercise testing in clinical medicine. [PMID: 11075788] Lancet. 2000;356:1592-7.[Medline]
12. Froelicher VF, Callaham PR, Angelo J, Lehmann KG. Treadmill exercise testing and silent myocardial ischemia. [PMID: 2681058] Isr J Med Sci. 1989;25:495-502.[Medline]
13. Blair SN, Kohl HW 3rd, Barlow CE, Paffenbarger RS Jr, Gibbons LW, Macera CA. Changes in physical fitness and all-cause mortality. A prospective study of healthy and unhealthy men. [PMID: 7707596] JAMA. 1995;273:1093-8.[Abstract]
14. O'Rourke RA, Brundage BH, Froelicher VF, Greenland P, Grundy SM, Hachamovitch R, et al. American College of Cardiology/American Heart Association Expert Consensus document on electron-beam computed tomography for the diagnosis and prognosis of coronary artery disease. [PMID: 10880426] Circulation. 2000;102:126-40.
15. Hopkirk JA, Leader S, Uhl GS, Hickman JR Jr, Fischer J. Limitation of exercise-induced R wave amplitude changes in detecting coronary artery disease in asymptomatic men. [PMID: 6693653] J Am Coll Cardiol. 1984;3:821-6.[Abstract]
16. Sox HC Jr, Garber AM, Littenberg B. The resting electrocardiogram as a screening test. A clinical analysis. [PMID: 2528311] Ann Intern Med. 1989;111:489-502.
17. Coplan NL, Fuster V. Limitations of the exercise test as a screen for acute cardiac events in asymptomatic patients. [PMID: 2321524] Am Heart J. 1990;119:987-90.[Medline]
18. Bild DE, Bluemke DA, Burke GL, Detrano R, Diez Roux AV, Folsom AR, et al. Multi-ethnic study of atherosclerosis: objectives and design. [PMID: 12397006] Am J Epidemiol. 2002;156:871-81.
19. Gibbons RJ, Balady GJ, Bricker JT, Chaitman BR, Fletcher GF, Froelicher VF, et al. ACC/AHA 2002 guideline update for exercise testing: summary article: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Committee to Update the 1997 Exercise Testing Guidelines). [PMID: 12356646] Circulation. 2002;106:1883-92.
20. American Academy of Family Physicians. Clinical Care and Research. Accessed at http://www.aafp.org/x10593.xml on 20 November 2003.
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